FDA Inspection 993764 — AgaMatrix, Inc.

AgaMatrix, Inc. — FEI 3004637226

The FDA completed an inspection of AgaMatrix, Inc. on Nov 21, 2016 in Derry, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 21, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Derry, NH (United States)

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